Allele Registry

Canonical Allele Identifier: PA891845284

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000688679

ClinVar Variation:

568349

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Thr1953Arg	CA382548478 NM_000051.4:c.5858C>G